WO2010127272A3 - Hydroxyethylamino sulfonamide derivatives - Google Patents
Hydroxyethylamino sulfonamide derivatives Download PDFInfo
- Publication number
- WO2010127272A3 WO2010127272A3 PCT/US2010/033206 US2010033206W WO2010127272A3 WO 2010127272 A3 WO2010127272 A3 WO 2010127272A3 US 2010033206 W US2010033206 W US 2010033206W WO 2010127272 A3 WO2010127272 A3 WO 2010127272A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sulfonamide derivatives
- compound
- hydroxyethylamino sulfonamide
- hydroxyethylamino
- compositions
- Prior art date
Links
- JKTOKCJLZBURKJ-UHFFFAOYSA-N 1-hydroxy-2-(sulfamoylamino)ethane Chemical class NS(=O)(=O)NCCO JKTOKCJLZBURKJ-UHFFFAOYSA-N 0.000 title abstract 2
- 241000725303 Human immunodeficiency virus Species 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
This invention relates to novel hydroxyethylamino sulfonamides, their derivatives, pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a compound with the ability to act as an HIV (human immunodeficiency virus) protease inhibitor.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21497709P | 2009-04-30 | 2009-04-30 | |
US61/214,977 | 2009-04-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2010127272A2 WO2010127272A2 (en) | 2010-11-04 |
WO2010127272A3 true WO2010127272A3 (en) | 2011-04-21 |
Family
ID=42244939
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2010/033206 WO2010127272A2 (en) | 2009-04-30 | 2010-04-30 | Hydroxyethylamino sulfonamide derivatives |
Country Status (2)
Country | Link |
---|---|
US (1) | US20100305173A1 (en) |
WO (1) | WO2010127272A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8592487B2 (en) * | 2007-10-26 | 2013-11-26 | Concert Pharmaceuticals, Inc. | Deuterated darunavir |
US20090131363A1 (en) * | 2007-10-26 | 2009-05-21 | Harbeson Scott L | Deuterated darunavir |
AR080375A1 (en) | 2010-03-05 | 2012-04-04 | Sanofi Aventis | PROCEDURE FOR THE PREPARATION OF 2- (CYCLOHEXIMETHYL) -N- {2 - [(2S) -1-METHYLPIRROLIDIN-2-IL] ETIL} -1,2,3,4-TETRAHYDROISOCHINOLINE- 7-SULFONAMIDE |
US20140213553A1 (en) * | 2011-05-03 | 2014-07-31 | Concert Pharmaceuticals Inc. | Carbamoylpyridone derivatives |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995026325A2 (en) * | 1994-03-25 | 1995-10-05 | Isotechnika Inc. | Enhancement of the efficacy of drugs by deuteration |
US20050267074A1 (en) * | 2004-05-07 | 2005-12-01 | Sequoia Pharmaceuticals | Resistance-repellent retroviral protease inhibitors |
US20090076138A1 (en) * | 2007-09-15 | 2009-03-19 | Protia, Llc | Deuterium-enriched darunavir |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5968942A (en) * | 1992-08-25 | 1999-10-19 | G. D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
PT810209E (en) * | 1992-08-25 | 2002-09-30 | Searle & Co | HYDROXYETHYLAMINO-SULFONAMIDES OF ALPHA- AND BETA-AMINOACIDOS UTEIS AS INHIBITORS OF RETROVIRAL PROTEASE |
US7141609B2 (en) * | 1992-08-25 | 2006-11-28 | G.D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
US6221335B1 (en) * | 1994-03-25 | 2001-04-24 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
US6440710B1 (en) * | 1998-12-10 | 2002-08-27 | The Scripps Research Institute | Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds |
PT1104760E (en) * | 1999-12-03 | 2003-06-30 | Pfizer Prod Inc | SULFAMOYL-HETEROARILPIRAZOLE COMPOUNDS AS ANALGESIC AND ANTI-INFLAMMATORY AGENTS |
EP1532127B1 (en) * | 2002-06-27 | 2006-09-27 | SmithKline Beecham Corporation | PREPARATION OF STEREOISOMERS OF (3ALPHA, 3ALPHA/BETA, 6ALPHA/BETA) HEXAHYDROFURO(2,3-b) FURAN-3-OL |
TW200413273A (en) * | 2002-11-15 | 2004-08-01 | Wako Pure Chem Ind Ltd | Heavy hydrogenation method of heterocyclic rings |
WO2005000249A2 (en) * | 2003-06-27 | 2005-01-06 | Smithkline Beecham Corporation | Preparation of chemical compounds |
RS51073B (en) * | 2003-12-23 | 2010-10-31 | Tibotec Pharmaceuticals Ltd. | Process for the preparation of (3r,3as,6ar)-hexahydrofuro│2,3-b│ furan-3-yl (1s,2r)-3-││(4-aminophenyl) sulfonyl│(isobutyl), amino │-1-benzyl-2-2hydroxypropilcarbamate |
EP1855672A4 (en) * | 2005-03-11 | 2011-11-30 | Glaxosmithkline Llc | Hiv protease inhibitors |
CA2624179A1 (en) * | 2005-10-06 | 2007-04-12 | Auspex Pharmaceuticals, Inc. | Deuterated inhibitors of gastric h+, k+-atpase with enhanced therapeutic properties |
US7750168B2 (en) * | 2006-02-10 | 2010-07-06 | Sigma-Aldrich Co. | Stabilized deuteroborane-tetrahydrofuran complex |
MX2009002398A (en) * | 2006-09-05 | 2009-03-16 | Schering Corp | Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis. |
US8592487B2 (en) * | 2007-10-26 | 2013-11-26 | Concert Pharmaceuticals, Inc. | Deuterated darunavir |
US20090131363A1 (en) * | 2007-10-26 | 2009-05-21 | Harbeson Scott L | Deuterated darunavir |
-
2010
- 2010-04-30 US US12/771,551 patent/US20100305173A1/en not_active Abandoned
- 2010-04-30 WO PCT/US2010/033206 patent/WO2010127272A2/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995026325A2 (en) * | 1994-03-25 | 1995-10-05 | Isotechnika Inc. | Enhancement of the efficacy of drugs by deuteration |
US20050267074A1 (en) * | 2004-05-07 | 2005-12-01 | Sequoia Pharmaceuticals | Resistance-repellent retroviral protease inhibitors |
US20090076138A1 (en) * | 2007-09-15 | 2009-03-19 | Protia, Llc | Deuterium-enriched darunavir |
Non-Patent Citations (1)
Title |
---|
MARC VERMEIR, SOPHIE LACHAU-DURAND, GEERT MANNENS, FILIP CUYCKENS, BART VA HOOF, ARAZ RAOOF: "Absorption, Metabolism, and Excretion of Darunavir, a New Protease Inhibitor, Administered Alone and with Low-Dose Ritonavir in Healthy Subjects", DMD FAST FORWARD, 24109, 8 January 2009 (2009-01-08), pages 1 - 54, XP002588463, DOI: 10.1124/dmd.108.024109 * |
Also Published As
Publication number | Publication date |
---|---|
WO2010127272A2 (en) | 2010-11-04 |
US20100305173A1 (en) | 2010-12-02 |
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